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Technology Process of 2-Methoxyethylmercury chloride

2-Methoxyethylmercury chloride

Base Information
  • Chemical Name:2-Methoxyethylmercury chloride
  • CAS No.:123-88-6
  • Molecular Formula:C3H7 Cl Hg O
  • Molecular Weight:295.131
  • Hs Code.:2931900090
  • European Community (EC) Number:204-659-7
  • Mol file:123-88-6.mol
2-Methoxyethylmercury chloride

Synonyms:Agallol 3;Agollol 3;Emisan 6;methoxyethylmercury chloride;neanthine;neanthine, 14C-labeled cpd

Suppliers and Price of 2-Methoxyethylmercury chloride
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Chemical Property of 2-Methoxyethylmercury chloride
Chemical Property:
  • Melting Point:115°C 
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA：9.23000 
  • Density:g/cm3 
  • LogP:1.28740 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:2
  • Exact Mass:295.989186
  • Heavy Atom Count:6
  • Complexity:26.8
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes:T,N 
  • Statements: 25-34-48/25-50/53 
  • Safety Statements: 36/37/39-45-60-61 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COCC[Hg]Cl
Technology Process of 2-Methoxyethylmercury chloride

There total 1 articles about 2-Methoxyethylmercury chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

MEMC
123-88-6

MEMC

Guidance literature:
Methyl-vinyl-ether;
DOI:10.1039/df9623400025

Reference yield: 44.0%

triiron dodecarbonyl
17685-52-8

triiron dodecarbonyl

MEMC
123-88-6

MEMC

thiophenol
108-98-5

thiophenol

(CH<sub>3</sub>OCH<sub>2</sub>CH<sub>2</sub>C(O))(C<sub>6</sub>H<sub>5</sub>S)Fe<sub>2</sub>(CO)6

(CH3OCH2CH2C(O))(C6H5S)Fe2(CO)6

Guidance literature:
With triethylamine; In tetrahydrofuran; addn. of thiol and Et3N to Fe3(CO)12 soln. (equim. amts., room temp., N2-atmosphere), addn. of Hg-compd., stirring (3 h); chromy. (SiO2, pentane);
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